Clinical Trial Manager

🕒 May 11

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Immatics

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2000

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Immatics is a biotechnology company focused on developing targeted immunotherapies for cancer patients, particularly in treating solid tumors. The company combines the discovery of cancer immunotherapy targets with the development of specific T cell receptors to enable a robust immune response. Immatics' pipeline includes Adoptive Cell Therapies and TCR Bispecifics, and it collaborates with global leaders in the pharmaceutical industry. The company's mission is to advance its therapies to improve the lives of cancer patients, and it maintains a strong commitment to innovation in immunotherapy technologies.

📋 Description

• Oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company SOPs. • Work closely with cross-functional teams and clinical sites to drive study execution, site engagement, and operational excellence across clinical trials. • Lead site feasibility, selection, initiation, and greenlight activities for clinical trial sites. • Develop and maintain study-specific operational plans, training materials, and monitoring documentation. • Oversee site management activities, including site engagement, regulatory submissions, and monitoring oversight. • Review trial progress, patient recruitment, and data quality metrics, and implement actions to support study objectives. • Provide guidance and oversight to CRAs, including trip report review and training support. • Manage protocol and GCP deviations and contribute to continuous improvement of clinical operations processes and procedures.

🎯 Requirements

• Bachelor’s degree in life sciences, nursing, or a related field • 2+ years of experience in on-site clinical monitoring and 2+ years of Clinical Trial Manager experience within the pharmaceutical or biotechnology industry • Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations • Demonstrated experience managing clinical trial sites, monitoring activities, and regulatory documentation • Proficiency with clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office)

🏖️ Benefits

• Competitive rates for Health, Dental, and Vision Insurance • 4 weeks of vacation, granted up front each year and prorated for first and last year of employment. • 12 company paid holidays • 7 days of sick time • 100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars • 100% employer-paid short- and long-Term disability coverage • 401(k) with immediate eligibility and company match… The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment. • Partially paid parental leave for eligible employees. • Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance.